U.S. patent number 5,376,114 [Application Number 08/015,246] was granted by the patent office on 1994-12-27 for cannula pumps for temporary cardiac support and methods of their application and use.
Invention is credited to Robert Jarvik.
United States Patent |
5,376,114 |
Jarvik |
December 27, 1994 |
Cannula pumps for temporary cardiac support and methods of their
application and use
Abstract
A cannula pump is provided which incorporates a miniature rotary
pump into a cardiac cannula of essentially the same size as
currently utilized with routine cardiopulmonary bypass. The pump
may be inserted via a single small incision in the heart to obtain
both inflow and outflow cannulation simultaneously, and provide
sufficient flow to completely unload the ventricle during its use.
Because application of the device is extraordinarily simplified, it
is suitable for rapid emergency insertion in any setting where the
chest can be safely opened, including emergency room and
battlefield applications. A small electric motor, implanted within
the heart, provides power to the impeller via a small shaft
supported on blood immersed bearings. A disposable cannula pump
utilized with a reusable motor provides an inexpensive device for
routine surgical use.
Inventors: |
Jarvik; Robert (New York,
NY) |
Family
ID: |
26687135 |
Appl.
No.: |
08/015,246 |
Filed: |
February 5, 1993 |
Related U.S. Patent Documents
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Application
Number |
Filing Date |
Patent Number |
Issue Date |
|
|
969034 |
Oct 30, 1992 |
|
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Current U.S.
Class: |
623/3.3; 600/16;
128/898; 623/3.13 |
Current CPC
Class: |
A61M
60/17 (20210101); A61M 60/414 (20210101); A61M
60/829 (20210101); A61M 60/422 (20210101); A61M
60/148 (20210101); A61M 60/205 (20210101); A61M
60/857 (20210101); A61M 60/82 (20210101); A61M
60/50 (20210101); A61M 60/135 (20210101); A61M
60/871 (20210101); A61M 2205/3334 (20130101); A61M
60/818 (20210101) |
Current International
Class: |
A61M
1/10 (20060101); A61M 1/12 (20060101); A61M
001/10 (); A61N 001/362 (); A61F 002/54 (); A61B
019/00 () |
Field of
Search: |
;623/1,2,3,66 ;600/16-18
;128/898 ;415/900 |
References Cited
[Referenced By]
U.S. Patent Documents
Primary Examiner: Green; Randall L.
Assistant Examiner: Burke; Elizabeth M.
Parent Case Text
This application is a continuation-in-part of Ser. No. 07/969,034
filed Oct. 30, 1992, now abandoned.
Claims
I claim:
1. A method of inhibiting binding or clogging malfunction caused by
blood or thrombus, of a temporary blood pump having blood immersed
pump impeller means, blood immersed pump impeller bearing means,
motor means, and motor bearing means comprising:
a. enclosing said motor bearing means in a chamber which is sealed
except at a single orifice of minimal area through which some blood
can pass and through which passes a small diameter shaft to convey
power from said motor means to said blood immersed pump impeller
means,
b. before blood pumping is begun, filling said chamber with fluid
in which said motor bearing means can operate,
c. providing a sufficient distance between said orifice and said
motor bearing means, such that only blood mixed with said fluid
reaches said motor bearing means during use of the temporary blood
pump,
d. and providing a sufficient volume of fluid in said chamber such
that blood entering therewithin is diluted by the fluid to inhibit
malfunction of the pump.
Description
FIELD OF THE INVENTION
This invention relates to circulatory support utilizing miniature
rotary blood pumps inserted into the heart for emergency use or
during heart surgery. The invention includes pumps mounted within
cannulae adapted for extremely simple application at surgery which
are capable of providing the entire pumping output required for
patient survival.
BACKGROUND OF THE INVENTION
Mechanical blood pumps are commonly applied to temporarily support
the pumping function of the heart during heart surgery or during
periods of heart failure. The most widely applied devices include
roller pumps and centrifugal pumps currently used in more than
400,000 cases of heart surgery annually. Usually, the pumps
comprise part of a cardiopulmonary bypass circuit in which many
components are combined including an oxygenator, a heat exchanger,
blood reservoirs and filters, and many feet of tubing to transport
the blood from the patient on the operating table to the heart-lung
machine located nearby and back to the patient. Blood is withdrawn
from the patient via uptake cannulae placed into the vena cavae and
atria or ventricles of the heart and pumped back into the pulmonary
artery and aorta via return cannulae. The system generally works
well but is complicated and expensive, exposes the blood to a high
surface area of foreign materials which causes damage, requires
full anticoagulation, and requires considerable time to set up and
manage by a skilled technician.
In most cases of coronary artery bypass surgery the heart is cooled
and stopped and an oxygenator is used although it is not necessary
to actually open the heart as it is with valve surgery. In a few
cases, the oxygenator is omitted from the system and the patients
own lungs continue to function during the course of the surgical
procedure. In such cases, either the pumping function of the left
ventricle alone or both the left and right ventricles, is supported
mechanically. Pulsatile pumps and continuous flow pumps have been
used experimentally and in human cases. The heart is not cooled and
is not stopped, although drugs may be given to slow its rate. The
procedure has a number of important advantages in appropriate
cases, however, present blood pumps, cannulae, and tubing sets have
not been developed specifically for this application, and setup,
cannulation, priming, and patient management during the procedure
are somewhat makeshift and leave room for considerable improvement.
The cannula pump of the present invention is especially suited to
this use, and greatly simplifies the procedure, reducing the number
of cannulation sites, reducing the surface area of foreign
materials, reducing the priming volume and setup time, and
permitting very simple management of heart function during the
procedure.
To support the systemic circulation, a single cannula containing a
miniature rotary pump is inserted into the heart, via a small
incision, and both the necessary inflow and outflow connections are
accomplished immediately. The blood pump may be inserted via the
apex of the ventricle, the atrium, or the aorta, but in each case
only one cannulation is necessary. The pump itself resides within
the cannula and is connected by a short drive shaft to a small
motor outside the heart, usually positioned immediately adjacent to
the heart in direct connection with the cannula. If support of the
pulmonic circulation is required, this is also achieved by a single
cannulation via the right ventricle, right atrium, superior vena
cava, or pulmonary artery. Thus, to support the total function of
the heart, two cannula pumps, each requiring only one cannulation
site, are used.
Cannula pumps are advantageous in cases requiring emergency
circulatory support where the chest can be rapidly opened for
access to the heart and the simple cannula pump can be inserted
immediately. Because no cumbersome or large equipment is involved,
the device can be applied in tight quarters, where use of larger
more complicated systems is precluded, and in cases of cardiac
arrest where there is inadequate time to setup and prime other
devices. Examples include ambulance, aircraft, emergency room,
cardiac cath lab, and rescue or military use in the field.
SUMMARY OF THE INVENTION
The present invention relates to miniature blood pumps utilized to
provide all or part of the pumping function of the heart during
cardiac surgery, during temporary periods of heart failure, and
during medical emergencies involving severe heart failure. The
device includes a miniature pump, such as an axial-flow or
mixed-flow pump mounted within a generally tubular cannula, similar
in size and shape to cannulae used to withdraw blood from the heart
or to return blood to the great vessels during routine heart-lung
machine utilization. However, the cannulae generally differ
functionally because, with the pump mounted within the cannula, a
single cannula is able to provide both the inflow and outflow
functions and therefore a single insertion site is sufficient, in
many cases. In some cases, such as where the patient has a
prosthetic valve which prevents passage of a cannula across it, two
cannulation sites may be used. The pumps of the present invention
may use blood-immersed mechanical bearings and the principles of
high-flow washing of the junction of the rotary and stationary
parts of the pump to prevent thrombus accumulation. These
principles together with the method of intraventricular
implantation are disclosed in my previous patents U.S. Pat Nos.
4,994,078 and 5,092,879. Although the present invention has much in
common with the inventions of these prior patents, basic
adaptations of the pump and motor bearing system are new as well as
the cannula type of device, its function, and its methods of use.
The present invention utilizes a small-diameter wire as a rotating
shaft which drives the pump impeller, compared to the stationary
wire of the previous devices. It is feasible for temporary use
since wear is minimal in a period of a few hours or even a few
weeks, compared to the permanent implant applications which require
durability of many years. Tension on the wire is not required, and
the wire is sufficiently stiff to impart the necessary rotary
torque without warping, breaking, or vibrating excessively. The
pumps are smooth and quiet during use and will not cause
significant blood damage if fabricated properly.
The present invention requires major surgery for its insertion and
differs from previous prior art inventions such as the
"HIGH-CAPACITY INTRAVASCULAR BLOOD PUMP UTILIZING PERCUTANEOUS
ACCESS" by Wampler, U.S. Pat. No. 4,625,712, in its structure and
function, as well as its intended use. The present cannula pump is
not suitable for percutaneous access, and is inserted via major
surgery for use during the surgical procedure, or for relatively
short term use following surgery. The invention of Wampler utilizes
a remote motor placed about a meter away from the pump and
connected to it via a long flexible shaft. The motor is located
outside the body whereas the motor used with the present invention
is implanted within the body and is directly coupled to the pump by
a short stiff shaft only a few centimeters long. This eliminates
the problem of flexible shaft breakage which has caused the FDA to
withdraw experimental approval to test the Wampler pump in human
patients. Since the present pump is not inserted through a long
small diameter blood vessel via an access site remote from the
heart, it is able to be large enough to support the entire cardiac
output, as roller pumps and centrifugal pumps utilized during
cardiac surgery typically must do. The Wampler pump is limited due
to the small diameter mandated by the remote insertion requirement
and can only provide a fraction of the blood flow necessary for
full support of the patient. Essentially the Wampler pump is a
remotely inserted assist pump, and the present invention is a
directly inserted, high flow, total cardiac output bypass pump.
Utilizing cannula pumps of the present invention, approximately 1.2
cm in diameter, blood flow up to 8 liters per minute is obtained
with 100 mm-Hg outflow pressure and rotational speed varying from
approximately 15,000 to 25,000 rpm, depending upon flow and
pressure. With flow in the range of 6 liters per minute and
pressure in the range of 80 mm-Hg, which represents a typical
operating condition, the power requirement for the system is below
15 watts. This permits battery operation for several hours with a
very compact and lightweight battery. The system may include a
simple control and display module which is small enough to be
sterilized and utilized in the sterile surgical field. It may also
incorporate microprocessor-based control and monitoring algorithms
to regulate the flow and pressure, or to display the flow and
pressure measured by sensors or calculated from comparison of
measurements of speed and power consumption to a known
database.
Cannulae may be provided with built-in pressure sensors or
flow-sensing devices such as a hot-wire anemometer or ultrasonic
flow probe, and may be configured such that the simple insertion of
the cannulae accomplishes complete instrumentation including
pressure and flow measurements at the appropriate locations.
Alternatively, the cannula pumps may be used with no flow and
pressure sensors and patient management can be accomplished by
other observations, such as the degree of expansion or collapse of
the left atrium during surgery and the adequacy of perfusion as
judged by the arterial blood gases.
The cannulae pumps are capable of being fabricated utilizing
primarily injection-molded, polymeric components, permitting
low-cost and disposability of the cannulae and pumps themselves.
The motors which provide rotary power to the shaft may be provided
in a reusable configuration or also maybe made very inexpensively
to permit them to be disposable. A completely disposable unit
incorporating both a disposable motor and pump together with the
cannulae is disclosed as one embodiment of the invention.
OBJECTS OF THE INVENTION
It is an object of the present invention to provide miniature
rotary blood pumps mounted within cannulae for insertion into the
heart to support its pumping function.
It is a further object of the invention to provide an extremely
simple method of cardiac support capable of rapid application in
medical emergencies.
It is a still further object of the invention to provide cannula
pumps which can be manufactured and sold at relatively low cost,
permitting routine disposable use.
It is another object of the invention to improve the art of heart
surgery, improve patient care, decrease morbidity and lower
hospital costs.
It is a further object of the invention to provide cannula pumps
that may be rapidly and effectively applied in emergency open chest
surgical procedures at remote locations away from a fully equipped
hospital operating room.
It is further object of the invention to provide cannula pumps
incorporating flow and pressure sensors and utilizing automatic
control modes.
It is a further object of the invention to provide methods of
operating the pump motor without rotary shaft seals and without the
need for a continuous supply of fluid for a flush seal.
It is a further object of the invention to provide simple cannula
pumps which may be coated with anticoagulants, thus avoiding or
diminishing the need for systemic anticoagulation.
It is a further object of the present invention to provide a system
of heart support which minimizes exposure of the blood to foreign
materials.
It is an additional object of the invention to provide inexpensive
disposable axial- or mixed-flow blood pumps suitable for use with
an oxygenator in the system.
These and other objects of the present invention will be more fully
understood by referring to the drawings and specific descriptions
in the following sections.
THE DRAWINGS
Certain preferred embodiments of the invention are illustrated in
the following figures:
FIG. 1 is a schematic illustration of the heart, partially in
section with the anterior wall of the right ventricle and part of
the pulmonary artery removed. Two cannula pumps are shown, one
inserted through the apex of the left ventricle, with the out-flow
across the aortic valve into the aorta and the other inserted
across the apex of the right ventricle with the outflow across the
pulmonic valve into the pulmonary artery.
FIG. 2 shows a longitudinal section of a cannula pump including the
motor module. The pump and motor are assembled for use.
FIG. 3 is a longitudinal section of the generally cylindrical
cannula and blood-pumping components contained therein. FIG. 3 is
an enlarged portion of the cannula pump system illustrated in FIG.
2.
FIG. 4 is a longitudinal section of a reusable motor and motor
housing. The disposable components of the cannula pump are not
shown.
FIG. 5 is a longitudinal section of the disposable components the
cannula pump illustrated in FIG. 2, showing all disposable
components with the exception the outflow cannula and including a
removable hypodermic needle for filling a fluid chamber within the
device.
FIG. 6 is a longitudinal section of a cannula pump having a
disposable motor disposed in a housing formed integral with the
cannula.
FIG. 7 is a longitudinal section of another embodiment of a cannula
pump showing a reusable motor and motor housing, and a disposable
pump with the cannula in position to be coupled to the rotating
shaft of the motor via a mechanical connector.
FIG. 8 is a longitudinal section of an embodiment of the invention
in which a small diameter motor having an outside diameter
approximately the same as the largest diameter of the pump is
incorporated within the cannula.
FIG. 9 is a schematic drawing of the heart and great vessels in
which a cannula pump similar to that shown in FIG. 8 has been
inserted into the left ventricle with the outflow cannula section
placed across the aortic valve into the aorta.
FIG. 10 is a schematic drawing of the heart showing a cannula pump
placed with the electric motor in the right atrium, and the pump
placed within the right ventricle, with the outflow cannula section
positioned across the pulmonic valve into the pulmonary artery.
FIG. 11 is another schematic illustration showing the left
ventricle and aorta, with the right ventricle removed. A cannula
pump is shown placed with the motor within the left ventricle and
the pump together with the outflow cannula section placed in the
aorta.
GENERAL DESCRIPTION OF THE INVENTION
It is common surgical procedure to insert a tube, generally known
as a cannula, into any of the various chambers of the heart or any
of the great vessels which bring blood to and carry blood away from
the heart. Cannulae of many sizes and shapes are used, including
flexible polymer tubes, wire-reinforced polymer tubes, and even
rigid metal tubes. Generally, these tubes must be small enough to
permit them to be inserted into the heart or great vessels with
minimal damage to the tissues and must be large enough to permit
sufficient blood flow given that a considerable pressure drop
occurs across small diameter tubes at higher flow rates, especially
when the tubes are long. In any system where a blood pump is used
to replace or assist in the function of one of the ventricles,
blood must be removed via a cannula from either the ventricle
itself or the inflow vessels leading to the ventricle and must then
pass through a pump which ejects it into one of the large
arteries.
The present invention provides pumps mounted inside the cannulae
themselves which has many advantages previously cited, including
greater simplicity of application to the patient, reduction in the
resistance to blood flow of long tubes, reduced exposure to foreign
materials, and ease of patient management. Cannula pumps may be
provided in numerous embodiments., may reside within the heart
itself, within the great vessels, or only a portion of the cannula
may be introduced into the vascular system and the pump may be
located outside the heart and beside it on the surgical field.
FIG. 1 is a generally schematic view of the heart showing two
cannula pumps inserted for support of both the left heart function
and the right heart function. The left ventricle, generally
indicated at 2, contains a miniature axial flow pump within a
cannula, and the right ventricle, indicated at 4, contains another
pump. The outflow portions of the cannulae deliver blood
respectively from the left ventricle 2 into the aorta 6, and from
the right ventricle 4 into the pulmonary artery 8. The cannula pump
in the right ventricle is driven by an electric motor, generally
located and shown at 10. The actual axial flow blood pumping
portion is indicated at 12, and the outflow tube which channels the
blood into the pulmonary artery is shown at 14. Thus, blood enters
through side holes as indicated by the arrows at 15, and directly
encounters the axial flow pump hydrodynamic elements. The passage
for the blood between the inflow position 15 and the outflow into
the pulmonary artery, generally indicated at 14, is very short and
offers both a relatively low resistance to flow and a small surface
area of artificial materials to which the blood is exposed.
Additionally, because the entire volume of blood within the cannula
pump remains within the vascular system itself, it is appropriate
to consider that the priming blood volume of this pump is
essentially zero. That is, no blood need be withdrawn from the
cardiovascular system to fill the pump and tubing circuit with this
embodiment.
A second cannula pump, inserted in the left ventricle, is powered
by an electric motor 16, and contains an axial flow pump within the
left ventricle 18 into which blood enters through side holes 22 as
indicated by the arrows. The blood is pumped out of the outflow
portion of the cannula 20 which carries the blood across the aortic
valve leaflets 24 and into the aorta 6. The right and left cannula
pumps together thus intake blood from both ventricles and pump the
blood into the two main arteries leaving the heart. The pump is
respectively inserted through a small incision in the apex of
either ventricle and held there by a purse-string suture as
indicated in FIG. 1 at 30, for the right-sided cannula pump, and
indicated at 28 for the left-sided pump. Since the pumps are
inserted with the patient's open chest and the heart is exposed,
the surgeon can readily feel the heart and easily ascertain that
the tip of the cannulae has passed across the proper valve and into
the aorta or pulmonary artery as desired, rather than across an
inflow valve and into the left atrium or right atrium, which would
be improper. The anatomy of the heart makes proper placement
relatively simple and it is almost a straight-line direct path from
the apex to the aorta. With cannula pumps inserted in the fashion
shown in FIG. 1, the outflow valve, that is the aortic valve or
pulmonary artery valve, is able to close around the outside of the
cannula permitting a sufficient seal to prevent major leakage back
from the artery into the respective ventricle. This increases the
effectiveness and efficiency of the pump because if the valve were
absent or incompetent, a considerable portion of the blood ejected
out of the cannula could flow directly back to the inflow side of
the pump effectively making a short circuit without being pumped
through the organs of the body as desired. However, even without
complete sealing of the aortic or pulmonary artery valves, a
considerable stream of blood is ejected from the cannula pump at
high flow to provide momentum to the column of blood in the vessel
and may provide a sort of jet-pump effect. Thus, it is possible to
create a cannula pump that is functionally effective even without a
cannula actually crossing the aortic or pulmonary artery valve if a
sufficiently high-velocity stream of blood is ejected by the tip of
a cannula pump within the ventricle and directed properly across
the valve orifice.
In some patients who have mechanical heart valves implanted in
either the aorta or pulmonary artery, it is not possible to pass a
cannula across the mechanical valve. In such cases, cannula pumps
may be used where the inflow into the pump is via the apex of the
ventricle or via the atrium and the outflow of the pump returns the
blood into the aorta or pulmonary artery via a second incision into
that blood vessel. In certain other situations, for example in
surgical procedures where the ventricular chambers of the heart
must be opened for the purposes of the operation, cannula pumps
that withdraw blood from the atria and return it to aorta or
pulmonary artery, are required rather than devices inserted into
the ventricular cavity.
FIG. 2 shows a longitudinal sectional view of the cannula pump.
Blood enters the axial flow pump section 18 through side holes 22,
and is ejected through the outflow cannula 20. The pump contains a
rigid, relatively elongated portion 32 which is passed across the
apex of the heart and serves as a support around which the heart
muscle is tied utilizing the purse-string suture. An electric motor
to provide power to the pump impeller is indicated at 16 and
contains motor windings and laminations 60, and a housing 62 with
an electric cable 68. FIG. 4 illustrates the housing containing the
windings and laminations of the motor for use in an embodiment such
as shown in FIG. 2 where the motor and housing are reusable and the
other complements of the cannula pump are disposable. The motor and
housing in FIG. 4 combine with the disposable pump and bearings
illustrated in FIG. 5 and an outflow cannula portion to yield the
complete operational device shown in FIG. 2.
Referring to FIG. 3, the general layout of an axial flow pump such
as may be used with many embodiments of the invention is shown.
Several axial flow pump impeller blades 38 are mounted on an
impeller hub 36 supported for rotation on a set of bearings 40, 42
and 44. The impeller is driven by a stiff rotating wire 34 which
transmits rotary mechanical energy produced by the electric motor
to the impeller. Still referring to FIG. 3, the impeller hub
rotating thrust bearing member 40 and shaft 34 are all bonded
together to form a single rotating unit. Shaft 34 extends into
stationary bearing 42 and is rotationally supported by it. Shaft 34
also passes through stationary bearing element 44 and is
rotationally supported by that bearing member. Rotating thrust
bearing member 40 is composed of a wear-resistant material similar
to the stationary bearing elements 42 and 44. At each end axially
it absorbs the thrust bearing load to maintain the axial position
of the impeller while it is rotating and to carry and transmit
thrust loads produced by the action of the impeller blades against
the bloodstream. The rotating thrust bearing member 40 translates
these loads to the stationary bearing members. Two small gaps 54
and 56 exist at each end of the rotating impeller hub. Blood enters
these paper-thin gaps and bathes the bearings, including the small
cylindrical gap between the shaft 34 and each of the stationary
bearing elements 42 and 44.
The rotating impeller is supported by the bearing elements in such
a fashion that there is a smooth, continuous line of flow across
the junction between the stationary and rotating components of the
pump at gaps 54 and 56. The blood enters the inflow side holes 22,
passes across the inflow stator blades 52, supported on the inflow
hub 47, smoothly crosses the gap between the inflow hub and the
impeller hub at 54, passes across the impeller blades 38 and the
impeller hub 36, and then smoothly passes across the gap 56 between
the rotating impeller hub and outflow stator hub 46 and finally
passes across the outflow stator blades 48 and then out of the pump
through the outflow cannula.
FIG. 5 shows the disposable cannula pump including the axial flow
pump bearings, drive shaft, and the motor magnet and motor magnet
bearings utilized to transmit torque magnetically from the windings
of the motor to the shaft. The elongated outflow cannula segment is
omitted in FIG. 5.
A slot 66 in the disposable portion of the cannula pump is
configured to receive a pin 64 (FIG. 4) as the motor is coupled to
the cannula. In the embodiment shown, this coupling is accomplished
by sliding the disposable cannula components shown in FIG. 5 into
the motor housing shown in FIG. 4 which results in the assembly
shown in FIG. 2. The pin and slot prevent the cannula from rotating
within the motor housing thereby permitting the rotational torque
to turn only the motor magnet and attached elements and not rotate
the entire cannula. The disposable components are retained in
proper connection to the reusable motor and housing components by
magnetic forces, by an interference fit, or by other mechanical
means.
Power to rotate the impeller is transmitted to the shaft 34 by the
magnet 70 which is bonded to the shaft 34 via an intermediary
hollow shaft 76. The motor magnet is caused to rotate by the
rotating electromagnetic fields produced by the surrounding motor
windings (60 in FIG. 2) and thus it is seen that in the embodiment
shown in FIG. 5 the entire end of the disposable portion of the
cannula pump containing the motor magnet may be sealed and thus
eliminate rotary mechanical shaft seals through which either air or
fluids could leak. The motor magnet 70 is supported by a pair of
bearings 72 and 74 via the shaft 76. These bearings may be any of a
number of suitable types, including fluid-lubricated sleeve-type
journal bearings, ball bearings, or hydrodynamic fluid film
bearings. Many materials are suitable for this application,
especially considering that the cannula pump is designed for
short-term use and the durability of the bearings need not be very
long. Note that in the embodiment illustrated in FIG. 5, the motor
magnet bearings 72 and 74 are located some distance from the pump
impeller bearings 42 and 44. The drive shaft 34 transverses an
elongated channel 58, and any blood which enters this chamber
through the narrow gap between the shaft 34 and the impeller
bearing 44 must travel the full length of this channel to reach the
motor magnet bearings. A elastomeric flexible sealing stopper 82 is
inserted into a hole in the end of the cannula near the motor
magnet bearings. This stopper may be punctured by a small
hypodermic needle 84 through which fluid can be injected into the
chamber containing the motor magnet and motor magnet bearings which
is in continuity with the chamber leading to the impeller bearing
44. Shortly prior to the use of the cannula pump in the patient an
appropriate fluid such as sterile heparinized saline or a
low-molecular-weight dextran solution is injected via hypodermic
needle 84 so as to completely fill the chamber surrounding the
motor magnet, motor magnet bearings, and shaft. Air that is present
in this chamber at the time the fluid is ejected is forced to exit
in the vicinity of the impeller through the narrow gap between the
shaft 34 and the bearing sleeve 44. If sleeve-type bearings are
used to support the motor magnet, such as shown in FIG. 5, a small
hole 78 may be included to facilitate passage of the fluid through
the bearings while the chamber is being filled. After the chamber
is completely filled, the hypodermic needle is withdrawn and the
stopper 82 seals the needle hole. Thereafter when the cannula pump
is inserted into the heart, blood fills the outflow section of the
cannula and the space surrounding the impeller and inflow and
outflow stator blades and a tiny amount of blood enters the gap
between the rotating impeller hub and stationary stator hubs. A
film of blood diffuses into the gap between the stationary impeller
bearings 42 and 44 and the rotating shaft 34. This blood mixes with
the anticoagulated fluid in the gap between bearing sleeve 44 and
shaft 34 and thus when the pump is turned on the bearing is
immersed in blood partly diluted by the anticoagulated fluid.
In the embodiment shown in FIG. 5 there is no mechanical lip seal
preventing blood from entering chamber 58 and ultimately reaching
the area of the motor magnet bearings. However, since the chamber
in which the motor magnet bearings are contained is rigid and
sealed and pre-filled with fluid prior to use of the pump in the
patient, blood cannot enter that chamber unless some of the fluid
already present is removed. Therefore exchange of fluid between the
bloodstream and the chamber is very limited and only a small amount
of blood diffuses or seeps into the chamber during the duration of
use of the cannula pump in the patient. This blood is highly
diluted and anticoagulated and therefore does not interfere with
the function of the motor bearings.
FIG. 6 shows an embodiment of the invention in which the electric
motor as well as the remainder of the cannula pump are all
integrated in one disposable unit. Disposable motor 92 is enclosed
in a polymeric housing 86 which is attached to the axial flow pump
section 18 at the inflow stator blade supports 88.
The embodiment shown in FIG. 6 functions very similarly to the
embodiment shown in FIG. 2 and has the advantage that the air gap
94 between the motor windings 92 and the motor magnet 90 can be
very small permitting high efficiency of the motor. As seen in FIG.
2, the air gap 96 must be larger when the motor is separable from
the cannula parts of the pump to accommodate the cannula wall. In
the configuration shown in FIG. 6, anticoagulated fluid may be
injected via the hypodermic needle into chamber 80 which
communicates with the elongated chamber 58 via the bore of the
motor. Fluid thus can be injected via the hypodermic needle and
completely fill the chambers containing the motor, motor bearings,
and shaft, and reach the blood contacting portion of the pump at
the impeller bearing 44.
FIG. 7 shows an additional embodiment of the invention in which the
motor may be reusable and provided in a sterilizable housing which
may be attached to a disposable portion of the catheter pump
containing the stators, impeller, and inflow and outflow openings
for the blood. Referring to FIG. 7, the motor 98 is encased in a
motor housing 100 and incorporates ball bearings 104 and 106
supporting a shaft 108 fixed to the motor magnet 102. The shaft is
sealed with a radial lip seal 110. The shaft has a cavity 114 which
is not round in cross section but another shape such as square or
rectangular and is adapted to receive a like-shaped shaft extension
112 which provides a coupling to transmit rotary torque from the
motor shaft 108 to the cannula pump shaft 34. In this configuration
the motor bearings and motor magnets are not surrounded by fluid
but rather are surrounded by air. Blood and other fluids are kept
out of the chamber in which the motor is housed by the rotary shaft
seal 110. Similarly, chamber 58 in the disposable part of the
device may remain filled with air rather than fluid because two
rotary shaft seals 122 and 124 are utilized to exclude fluids.
Thus, prior to operation of the embodiment shown in FIG. 7, the
cannula portion is affixed to the motor portion by inserting the
shaft 112 into the hole 114 and pressing the end of the cannula 118
into the hole 120 in the end of the motor housing. The parts may be
thus attached together by an interference friction fit or other
methods of retention may be provided, such as a screw-on connector.
The function of the blood pump impeller, stators, and pump impeller
bearings is very similar to that described for the embodiment shown
in FIG. 3, with the bearings immersed in blood which enters the
narrow gaps between the rotating and stationary parts.
FIG. 8 illustrates a cannula pump in which a motor 126 is utilized
which is of small enough diameter to be inserted through a small
incision in the heart., such as in the apex. Such a motor,
approximately 12 mm in diameter by 22 mm long, provides sufficient
power to pump the entire normal workload of the left ventricle, and
sufficiently powerful motors can be made even smaller. The motor
receives electric power through wires 156 which enter the heart via
a cable 158 which passes across the wall of the ventricle and is
sealed by a purse string suture 28 or may pass across the wall of
the heart at another location. The rotor of the motor 128 is
supported by bearings 130 and 132 and is connected to the pump
impeller hub 134 which supports the impeller blades 136 by a small
diameter shaft 133. In the present embodiment, a rotary shaft seal
142 prevents blood from entering the motor and motor bearing
housing 127. Additional blood immersed bearings, 138 and 140 are
provided to support the shaft within the blood stream. Bearing 138
is supported in the motor housing and bearing 140 is supported by
the hub of the outflow stator 136 which in turn is supported by
outflow stator blades 137 within the pump housing 148. Thus, when
power is applied to rotate the motor rotor the rotary mechanical
power it provides is transferred to the impeller via the rotating
shaft 133. the action of the rotor blades against the blood draws
blood into the pump via inflow openings 150 and 152 and pumps the
blood through the outflow cannula 153 and out of the outflow
opening 154.
FIG. 9 shows a cannula pump inserted into the left ventricle 2 at
the apex and retained in place temporarily by a purse string suture
128. The power cable 158 protrudes from the apex and connects to
the motor controller and electric power source (not shown). This
embodiment is advantageous compared to that shown in FIG. 1 in
which the motor located outside the heart can interfere with the
surgeon's other tasks, such as suturing coronary artery bypass
grafts.
FIG. 10 shows another embodiment in which the device is inserted
across the wall of the right atrium and affixed in place by a purse
string suture 29. The device utilizes a motor 160 which is within
the right atrium 164, connected to the pump impeller, 168 by a
flexible shaft 166 and also a small diameter rigid shaft 135. This
shaft is supported on blood immersed bearings (not shown) in a
fashion similar to the pump of FIG. 8. The pump is enclosed in a
pump housing 170 which is located in the left ventricle and the
blood is pumped across an outflow cannula through the aortic valve
24 and is discharged into the aorta at 172. This separation of the
motor and pump has the advantage that there is a long distance for
blood to diffuse from the pump to the motor for embodiments that do
not use a rotary shaft seal. Similarly, an embodiment similar to
that shown in FIG. 10 can be applied with the motor in the left
atrium and the pump in the left ventricle.
FIG. 11 shows another embodiment similar to that shown in FIG. 8 in
which the pump housing 148 is elongated sufficiently to permit the
pump 136 to be in the aorta while the motor 126 is in the
ventricle. The rotating shaft 133 transmits power across the aortic
valve 24 to the pump impeller.
Additional embodiments of the cannula pump invention include
embodiments in which the cannula pump is provided with two separate
flexible polymeric tubular extensions to permit insertion of one as
an inflow and the other as an outflow tube. Thus without departing
from the scope of the above defined invention, numerous other
useful embodiments may be provided.
The information disclosed in the description of the present
invention is intended to be representative of the principles that I
have described. It will thus be seen that the objects of the
invention set forth above and those made apparent from the
preceding description are efficiently obtained and that certain
changes may be made in the above articles and constructions without
departing from the scope of the invention. It is intended that all
matter contained in the above description or shown in the
accompanying drawings shall be interpreted as illustrative but not
in a limiting sense. It is also understood that the following
claims are intended to cover all of the generic and specific
features of the invention herein described and all statements of
the sconce of the invention which as a matter of language might be
said to fall there between.
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